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Published on: February 17, 2014
A comparative study of transfusion-acquired human immunodeficiency virus-infected children with and without
D Gleason-Morgan1, J A Church, L A Ross
1Division of Allergy-Clinical Immunology, Childrens Hospital Los Angeles 90027.
Abstract:
For identification of the features of disseminated Mycobacterium avium complex (DMAC) in human immunodeficiency virus (HIV)-infected children, a retrospective medical record review of 31 long-term survivors with transfusion-acquired HIV was conducted. Nine patients developed DMAC defined as positive isolation of M. avium complex from peripheral blood. DMAC was diagnosed in patients 51 to 132 months of age (mean, 101). The time from HIV-infecting transfusion to DMAC diagnosis ranged from 37 to 132 months (mean, 92) and survival from the time of DMAC diagnosis ranged from 4 to 21 months (mean, 10). Selected laboratory and clinical measures in DMAC-positive and DMAC-negative subjects were compared. DMAC-positive patients had significantly lower CD4+ T cell counts and higher HIV p24 antigen concentrations than DMAC-negative patients at comparable times. Increased percentages of circulating leukocyte band forms and increased aspartate aminotransferase values were seen more often in DMAC-positive patients. Fever and abdominal pain were the only clinical features seen more often in DMAC-positive than in DMAC-negative patients. At the end of the study period overall survival of DMAC-positive patients was less than that of DMAC-negative children, at 33% vs. 73%. DMAC occurs in profoundly immunocompromised children with advanced HIV disease and significantly affects survival. The clinical and laboratory features of DMAC are relatively nonspecific and a high index of suspicion in patients with markedly reduced CD4+ T cells is essential.
Insights
Disseminated Mycobacterium avium complex (DMAC) in children with advanced HIV disease is associated with significantly lower survival rates. Early identification requires a high index of suspicion due to nonspecific clinical and laboratory features.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- HIV/AIDS Research
Background:
- Disseminated Mycobacterium avium complex (DMAC) is a significant opportunistic infection in individuals with advanced human immunodeficiency virus (HIV) disease.
- Understanding the specific features of DMAC in pediatric populations is crucial for timely diagnosis and management.
Purpose of the Study:
- To identify the clinical and laboratory features distinguishing disseminated Mycobacterium avium complex (DMAC) in human immunodeficiency virus (HIV)-infected children.
- To assess the impact of DMAC on survival in this vulnerable pediatric cohort.
Main Methods:
- Retrospective medical record review of 31 long-term survivors with transfusion-acquired HIV.
- Comparison of laboratory markers (CD4+ T cell counts, HIV p24 antigen, aspartate aminotransferase) and clinical signs (fever, abdominal pain) between DMAC-positive and DMAC-negative patients.
Main Results:
- Nine patients developed DMAC, diagnosed between 51-132 months of age.
- DMAC-positive patients exhibited significantly lower CD4+ T cell counts and higher HIV p24 antigen levels.
- Fever and abdominal pain were more frequent in DMAC-positive children; overall survival was lower (33% vs. 73%).
Conclusions:
- DMAC occurs in profoundly immunocompromised children with advanced HIV disease, significantly impacting survival.
- Clinical and laboratory features of DMAC are nonspecific, necessitating a high index of suspicion in patients with severely reduced CD4+ T cells.
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